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AMG 193, Methylthioadenosine (MTA) Cooperative Protein Arginine Methyltransferase 5 (PRMT5) Inhibitor, Alone and in Combination With Docetaxel in Advanced Methylthioadenosine Phosphorylase (MTAP)-Null Solid Tumors

Clinicaltrials.gov ID

NCT05094336

Status

Recruiting

Study Type

Interventional, Phase 1/2

Sponsor

Amgen

Start Date

February 1, 2022

Anticipated End Date

February 27, 2026

Study Contact

Name: Amgen Call Center

Phone Number:866-572-6436

Email: medinfo@amgen.com

About the Study

The primary objective of Parts 1 and 2 of this study is to evaluate the safety, tolerability, and to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) of AMG 193 alone and in combination with docetaxel in adult participants with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-null solid tumors.

The primary objective of Part 3 of this study is to evaluate the objective response rate (ORR) of AMG 193 in adult participants with metastatic or locally advanced MTAP-null solid tumors.

Conditions

  • Advanced MTAP-null Solid Tumors

Inclusion/Exclusion Criteria?

Primary, Secondary, Other Outcome Measures??

Locations in Canada

  • Cross Cancer Institute, Edmonton, Alberta, T6G 1Z2, Canada

  • Princess Margaret Cancer Centre, Toronto, Ontario, M5G 2M9, Canada

About the Study

The primary objective of Parts 1 and 2 of this study is to evaluate the safety, tolerability, and to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) of AMG 193 alone and in combination with docetaxel in adult participants with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-null solid tumors.

The primary objective of Part 3 of this study is to evaluate the objective response rate (ORR) of AMG 193 in adult participants with metastatic or locally advanced MTAP-null solid tumors.

Conditions

  • Advanced MTAP-null Solid Tumors

Interventions

DRUG:

  • AMG 193

  • Docetaxel

  • Comparator AMG 193 Test Tablet

Locations in Canada

  • Cross Cancer Institute, Edmonton, Alberta, T6G 1Z2, Canada

  • Princess Margaret Cancer Centre, Toronto, Ontario, M5G 2M9, Canada

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The Canadian Cholangiocarcinoma Collaborative (C3) is supported by a Canadian Cancer Society Breakthrough Team Grant in partnership with the Canadian Institutes of Health Research. The granting funds for C3 are managed by The Ottawa Hospital Research Institute, which serves as the lead institute for all collaborative operations.

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